Help Me Support The GFPD

As many of you know, Archer was diagnosed with a Peroxisomal Biogenesis Disorder when he was 18 months after a long year of testing. This was a scary time for us, with a heartbreaking diagnosis for our little boy, but the Global Foundation for Peroxisomal Disorders (GFPD) was there to provide us with support from the very beginning. Over the years, the GFPD has provided us with educational programs, family conferences, and invaluable connection to other families also affected by PBD. In addition, the GFPD funds research and coordinates scientific collaboration worldwide. To us, the GPFD represents hope for a better future for Archer and others affected by this devastating disorder. Please join us for the 2021 Walk-Run-Ride to support the important work of the GFPD!